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首页> 外文期刊>Cytogenetic and genome research >Global gene expression profile after Salmonella enterica Serovar enteritidis challenge in two F8 advanced intercross chicken lines.
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Global gene expression profile after Salmonella enterica Serovar enteritidis challenge in two F8 advanced intercross chicken lines.

机译:沙门氏菌肠炎沙门氏菌肠炎沙门氏菌攻击后在两个F8先进的交叉鸡系中的全球基因表达谱。

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摘要

A chicken 13K cDNA microarray was used to profile global gene expression after Salmonella enteritidis (SE) challenge of young chickens. Two F8 advanced intercross lines (AIL), broiler by Leghorn, and broiler by Fayoumi, were studied. Day-old chicks were orally inoculated with SE, and spleens were harvested at day 7 or 8 post-inoculation. The SE bacteria burden in the spleen was quantified. The 20% high and 20% low SE burden birds within each AIL and harvest time were studied by microarray. The loop design was used for pair-comparison between high and low SE burden challenged birds and unchallenged birds, within each AIL and harvest time. The signal intensity of each gene was globally normalized and expressed on the natural log scale. A mixed model including line, treatment, time, array (random effect), dye, and all two-way interactions among treatment, time, and line was used to identify differentially expressed candidate genes at the 1% significance level. The results suggest that genetics, time, and interaction between genetics and time play important roles in gene regulation of SE infection and colonization in chickens. The differentially expressed genes identified in the current study are candidates for detailed hypothesis-driven investigation of genes determining resistance to SE in chickens.
机译:鸡13K cDNA微阵列用于分析雏鸡肠炎沙门氏菌(SE)攻击后的全局基因表达。研究了两个F8先进的杂交系(AIL),分别是来格霍恩(Leghorn)的肉鸡和法尤米(Fayoumi)的肉鸡。对一天大的雏鸡进行口服SE接种,并在接种后第7或8天收获脾脏。定量脾中的SE细菌负荷。通过微阵列研究了每个AIL和收获时间中20%高SE和20%低SE的家禽。循环设计用于在每个AIL和收获时间之内对SE负担高的挑战鸟类和未挑战的鸟类进行高低配对。每个基因的信号强度已全局标准化,并以自然对数刻度表示。使用包括品系,处理,时间,阵列(随机效应),染料以及处理,时间和品系之间所有双向相互作用的混合模型,以1%的显着性水平鉴定差异表达的候选基因。结果表明,遗传,时间以及遗传与时间之间的相互作用在鸡SE感染和定居的基因调控中起着重要作用。在当前研究中鉴定出的差异表达基因是详细的假设驱动研究,用于确定鸡对SE的抗性的基因。

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